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本文引用的文献

1
In vitro microvessels for the study of angiogenesis and thrombosis.用于研究血管生成和血栓形成的体外微血管。
Proc Natl Acad Sci U S A. 2012 Jun 12;109(24):9342-7. doi: 10.1073/pnas.1201240109. Epub 2012 May 29.
2
Microfluidic models of vascular functions.血管功能的微流控模型。
Annu Rev Biomed Eng. 2012;14:205-30. doi: 10.1146/annurev-bioeng-071811-150052. Epub 2012 Apr 23.
3
A practical method for patterning lumens through ECM hydrogels via viscous finger patterning.一种通过粘性指状图案化在细胞外基质水凝胶中形成管腔的实用方法。
J Lab Autom. 2012 Apr;17(2):96-103. doi: 10.1177/2211068211426694. Epub 2012 Jan 24.
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Microscale functional cytomics for studying hematologic cancers.用于研究血液系统癌症的微尺度功能细胞组学
Blood. 2012 Mar 8;119(10):e76-85. doi: 10.1182/blood-2011-10-384347. Epub 2012 Jan 18.
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Fluid forces control endothelial sprouting.流体力控制着内皮细胞的发芽。
Proc Natl Acad Sci U S A. 2011 Sep 13;108(37):15342-7. doi: 10.1073/pnas.1105316108. Epub 2011 Aug 29.
6
High-throughput analysis of single hematopoietic stem cell proliferation in microfluidic cell culture arrays.微流控细胞培养芯片中单造血干细胞增殖的高通量分析。
Nat Methods. 2011 May 22;8(7):581-6. doi: 10.1038/nmeth.1614.
7
A microfluidic membrane device to mimic critical components of the vascular microenvironment.一种用于模拟血管微环境关键组件的微流控膜装置。
Biomicrofluidics. 2011 Mar 30;5(1):13409. doi: 10.1063/1.3530598.
8
Microfluidic cell culture and its application in high-throughput drug screening: cardiotoxicity assay for hERG channels.微流控细胞培养及其在高通量药物筛选中的应用:hERG通道的心脏毒性测定
J Biomol Screen. 2011 Jan;16(1):101-11. doi: 10.1177/1087057110386218. Epub 2010 Dec 3.
9
A microfluidic platform for complete mammalian cell culture.一种用于完整哺乳动物细胞培养的微流控平台。
Lab Chip. 2010 Jun 21;10(12):1536-42. doi: 10.1039/c002147d. Epub 2010 Apr 15.
10
Automated high-throughput microchannel assays for cell biology: Operational optimization and characterization.用于细胞生物学的自动化高通量微通道分析:操作优化与表征
JALA Charlottesv Va. 2010 Feb 1;15(1):25-32. doi: 10.1016/j.jala.2009.10.002.

无管微流控血管生成分析检测方法,结合了三维内皮衬里微血管。

Tubeless microfluidic angiogenesis assay with three-dimensional endothelial-lined microvessels.

机构信息

Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI 53706, USA.

出版信息

Biomaterials. 2013 Feb;34(5):1471-7. doi: 10.1016/j.biomaterials.2012.11.005. Epub 2012 Nov 26.

DOI:10.1016/j.biomaterials.2012.11.005
PMID:23191982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3529167/
Abstract

The study of angiogenesis is important to understanding a variety of human pathologies including cancer, cardiovascular and inflammatory diseases. In vivo angiogenesis assays can be costly and time-consuming, limiting their application in high-throughput studies. While traditional in vitro assays may overcome these limitations, they lack the ability to accurately recapitulate the main elements of the tissue microenvironment found in vivo, thereby limiting our ability to draw physiologically relevant biological conclusions. To bridge the gap between in vivo and in vitro angiogenesis assays, several microfluidic methods have been developed to generate in vitro assays that incorporate blood vessel models with physiologically relevant three-dimensional (3D) lumen structures. However, these models have not seen widespread adoption, which can be partially attributed to the difficulty in fabricating these structures. Here, we present a simple, accessible method that takes advantage of basic fluidic principles to create 3D lumens with circular cross-sectional geometries through ECM hydrogels that are lined with endothelial monolayers to mimic the structure of blood vessels in vitro. This technique can be used to pattern endothelial cell-lined lumens in different microchannel geometries, enabling increased flexibility for a variety of studies. We demonstrate the implementation and application of this technique to the study of angiogenesis in a physiologically relevant in vitro setting.

摘要

血管生成的研究对于理解包括癌症、心血管和炎症性疾病在内的多种人类病理生理学非常重要。体内血管生成测定法可能既昂贵又耗时,限制了它们在高通量研究中的应用。虽然传统的体外测定法可能克服这些限制,但它们缺乏准确重现体内组织微环境的主要元素的能力,从而限制了我们得出生理相关生物学结论的能力。为了弥合体内和体外血管生成测定法之间的差距,已经开发了几种微流控方法来生成体外测定法,该方法将具有生理相关三维(3D)管腔结构的血管模型与体外测定法相结合。然而,这些模型并没有得到广泛采用,这在一定程度上可以归因于制造这些结构的困难。在这里,我们提出了一种简单、可及的方法,该方法利用基本的流体原理,通过 ECM 水凝胶创建具有圆形横截面几何形状的 3D 管腔,该水凝胶内衬有内皮单层细胞,以模拟体内血管的结构。该技术可用于对不同微通道几何形状的内皮细胞衬里管腔进行图案化,为各种研究提供更大的灵活性。我们展示了该技术在生理相关体外环境中血管生成研究中的实施和应用。